Literature DB >> 10506170

Bipartite modular structure of intrinsic, RNA hairpin-independent termination signal for phage RNA polymerases.

Y S Kwon1, C Kang.   

Abstract

The phage SP6 RNA and T7 RNA polymerases, which are closely related to each other, intrinsically stop at two signals in the Escherichia coli rrnB terminator t1 through different mechanisms. The downstream signal functioned without an RNA secondary structure formation, in which the signal was still active when separated from the upstream, hairpin-forming signal, and IMP incorporation enhanced its efficiency. The sequence from -15 to -1 was essential for the downstream, hairpin-independent termination (at -1). The results of SP6 transcription with heteroduplex templates and ribonucleotide analogs suggested that the downstream signal consists of two functionally different modules. The effects of iodo-CMP or IMP incorporation into RNA on termination efficiency were not sensitive to incorporation at -9 and upstream, but they were reactive to incorporation at -6 and -2, as reflected by strong iodo-rC:dG and weak rI:dC base pairing. Thus, the downstream module (from -8 approximately -6 to -1) appears to facilitate the release of RNA. Mismatches in the templates at -6 to +1 allowed for efficient termination, unlike those upstream of the sequence. The upstream module (from -15 to -9 approximately -7) functions as a duplex. Pausing of the SP6 elongation complex at the termination site was detected when RNA release was suppressed by the incorporation of 5-bromo-UMP, and it was dependent on the upstream module. Results of single-round SP6 transcriptions using 3'-deoxynucleotides and immobilized templates indicated that RNA was not released from the elongation complexes halted at the termination site on the template variants carrying mutations in the upstream or downstream module, whereas such complexes on the wild type template were dissociated. Thus, halting or simple pausing was not sufficient for termination even when the downstream module was intact. The upstream module appears to mediate such conformation change necessary for termination.

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Year:  1999        PMID: 10506170     DOI: 10.1074/jbc.274.41.29149

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  DNA sequencing and genotyping by transcriptional synthesis of chain-terminated RNA ladders and MALDI-TOF mass spectrometry.

Authors:  Y Kwon; K Tang; C Cantor; H Köster; C Kang
Journal:  Nucleic Acids Res       Date:  2001-02-01       Impact factor: 16.971

2.  Sequential multiple functions of the conserved sequence in sequence-specific termination by T7 RNA polymerase.

Authors:  Younghee Sohn; Changwon Kang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-22       Impact factor: 11.205

3.  Probing conformational changes in T7 RNA polymerase during initiation and termination by using engineered disulfide linkages.

Authors:  Kaiyu Ma; Dmitry Temiakov; Michael Anikin; William T McAllister
Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

4.  Mechanism of T7 RNAP pausing and termination at the T7 concatemer junction: a local change in transcription bubble structure drives a large change in transcription complex architecture.

Authors:  Dhananjaya Nayak; Sylvester Siller; Qing Guo; Rui Sousa
Journal:  J Mol Biol       Date:  2007-12-04       Impact factor: 5.469

5.  Characterization of 582 natural and synthetic terminators and quantification of their design constraints.

Authors:  Ying-Ja Chen; Peng Liu; Alec A K Nielsen; Jennifer A N Brophy; Kevin Clancy; Todd Peterson; Christopher A Voigt
Journal:  Nat Methods       Date:  2013-06-02       Impact factor: 28.547

6.  A single mutation attenuates both the transcription termination and RNA-dependent RNA polymerase activity of T7 RNA polymerase.

Authors:  Hui Wu; Ting Wei; Bingbing Yu; Rui Cheng; Fengtao Huang; Xuelin Lu; Yan Yan; Xionglue Wang; Chenli Liu; Bin Zhu
Journal:  RNA Biol       Date:  2021-07-27       Impact factor: 4.766

7.  Engineering efficient termination of bacteriophage T7 RNA polymerase transcription.

Authors:  Diana G Calvopina-Chavez; Mikaela A Gardner; Joel S Griffitts
Journal:  G3 (Bethesda)       Date:  2022-05-30       Impact factor: 3.542

  7 in total

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